Cationic conductor, its intermediate, and lithium secondary battery using the conductor

ABSTRACT

The disclosure discloses a polymer represented by the general formula, 
                         
wherein R p  is a residue of a polymer of a compound having a polymerizable unsaturated bond, Q is an organic residue of n+1 valences and connected directly or through another group to R p  by means of a single bond, M k+  is a cation of k valence, Z is an organic function group capable of forming an ionic bond with cation M k+  or an organic function group having a coordination capability with M k+ , and m, n and k are integers of one or more. The disclosure also discloses an intermediate of the polymer mentioned above.

This application is a Divisional application of application Ser. No.10/392,921, filed Mar. 21, 2003, now U.S. Pat. No. 7,300,991 thecontents of which are incorporated herein by reference in theirentirety.

DESCRIPTION OF THE INVENTION

1. Field of the Invention

The present invention relates to an ionic conductive organic electrolyteand a polymer electrolyte.

2. Prior Art

As the progress of electronic technology, performance of electronicdevices has increased to make small sizes of them and make them potable,and then secondary batteries having high energy density for powersources of the devices are desired.

In responding to this demand, lithium ion secondary batteries with anorganic electrolyte solution (hereinafter referred to as lithiumbattery) that have remarkably increased energy density have beendeveloped and used widely.

In general, lithium batteries use as positive active material a lithiummetal complex oxide such as lithium cobalt composite oxide, for example,and as a negative active material a carbon material that is capable ofinserting lithium ions into intercalation of the carbon material (i. e.formation of lithium intercalation compound) and of releasing lithiumions from the intercalation.

As lithium batteries use as an electrolyte an inflammable organicelectrolyte, it is becoming difficult to secure safety of the batteriesas the energy density increases, when they are subjected to such heavyduty as overcharge and overdischarge. Then, lithium batteries that havelithium ion conductive solid polymers have developed, instead of theinflammable organic electrolyte solution.

Among the lithium ionic conductive solid polymers for the polymerelectrolytes, polyethylene oxide is a typical one. The possibility ofpolyethylene oxide as a lithium ionic conductive solid electrolyte ispointed out by Almand, et al in “First Ion Transport in Solids”, pp.131, Eselvier, New York, 1979.

There are many improvements of the polymers and investigations on otherpolymers. At present, an ionic conductive polymer that exhibits thehighest ionic conductivity is a copolymer of branched ethylene oxide andpropylene oxide as disclosed in Japanese Patent Laid-open 2000-123632.The ionic conductivity is about 10⁻⁴ Scm⁻¹.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 shows a graph that shows relationship between ionic conductivityof the polymer electrolyte and temperatures.

FIG. 2 shows a sectional view of a lithium battery that uses the polymerelectrolyte obtained in the procedure described later.

DESCRIPTION OF THE INVENTION

In the ionic conductive polymers that have been investigated heretofore,ion conductivity takes place jointly with molecular motion of thepolymer. That is, functional groups having coordinating capabilitypresent in the polymer chain make coordination to lithium ions, wherebylithium ions can move to other coordination groups by transition alongwith motion of molecular chains. Therefore, the ionic conductivitydepends on mobility of the molecular chains, and also depends on amotion necessary for conformation change of a main chain such asdihedral angle motion that needs large activation energy. When atemperature is low where the molecular motion is suppressed, ionicconductivity decreases at the same time.

The inventors have devised to employ as a mechanism for transferringions by the rotation of a single bond in a molecular chain that hassmall activation energy and that does not depend on motion of amolecular chain. In a compound, an organic compound having functionalgroups that can become coordination groups or ligands to lithium ionsare bonded to other organic groups, whereby the single bond can rotatefreely over the wide range of temperature. Exchange of lithium ionsbetween adjoining similar or analogous functional groups takes place bythe action of the rotation. This phenomenon brings about ionicconductivity.

Another manner was devised by the inventors. The structure of organicgroups having functional groups to be ligands of lithium ions that areconnected by means of the single bond was provided with such functionalgroups as amide groups. The groups form hydrogen bonds having stablestereo structure with ligands, and the pKa of the functional groups tobe ligands was changed to control coordination capability of lithiumions.

As a result, transition of lithium ions is accelerated from thefunctional groups of lower coordination capability to functional groupsof higher coordination groups. When employing this mechanism, higherionic conductivity is obtained even at such a low temperature thatsegmental motion of the polymer is suppressed.

The lithium-ion conductive polymer electrolyte of the present inventionshown in FIG. 2 comprises polymer and lithium salt. The polymerelectrolyte can be prepared by polymerizing monomer in the presence ofthe lithium salt both of them being dissolved in an organic solvent,followed by removing the solvent. The polymer electrolyte can beprepared by adding the lithium salt to the polymer solution dissolved inan organic solvent, followed by removing the solvent.

The form of the polymer electrolyte is a sheet form when it is used asan electrolyte of a lithium battery. The sheet also works as a separatorbetween anode and cathode electrodes. The sheet polymer electrolyte isprepared by casting a solution of a monomer and a lithium salt onpolytetrafluoroethylene (PTFE) sheet. Then, the monomer is polymerizedby heating addition polymerization, polyaddition polymerization,polycondensation polymerization, etc, followed by removing the solvent.

The sheet polymer electrolyte can also be prepared by casting a solutioncomprising a polymer and a lithium salt on the PTFE sheet, followed byremoving the solvent.

Organic solvents for dissolving the polymers and lithium salts are NMP,dimethylformamide, toluene, etc. which can solve the lithium salts anddo not react with the polymer.

The battery shown in FIG. 2 is assembled in a casing 4 in such a mannerthat the polymer electrolyte sheet 3 is sandwiched between an anode 2made of active material and a cathode 1 made of active material.

In order to make an intimate contact between the anode and the sheetelectrolyte and between the cathode and the sheet electrolyte, an anodeand cathode that comprise the polymer electrolyte are preferable. Inthis case, a monomer containing lithium salt dissolved in an organicsolvent is polymerized by heating on the anode and/or cathode. Asolution in which the polymer and lithium salt are dissolved in anorganic solvent is cast on the anode and/or cathode, followed byremoving the solvent.

Detailed Description of the Preferred Embodiments

The present invention will be described in detail by way of examples.

The polymer according to the present invention is represented by thegeneral formula,

wherein R_(p) is a residue of a polymer of a compound having apolymerizable unsaturated bond, Q is an organic residue of n+1 valencesand connected directly or through another group to R_(p) by means of asingle bond, M^(k+) is a cation of k valence, Z is an organic functiongroup capable of forming an ionic bond with cation M^(k+) or an organicfunction group having a coordination capability with M^(k+), and m, nand k are integers of one or more.

The intermediate of the polymer defined above is represented by thegeneral formula (I):

wherein R is a residue of a compound having a polymerizable unsaturatedbond, and Q, Z, M^(k+).m, n and k are the same as defined above.

The formula I represents a salt, wherein R is an organic group of an mvalence, Q is an organic group of an n+1 valence, Z is an anionicresidue of one valence, M⁺ is a cation of one valence, n and m areintegers of 1 or more. The group Q having an anionic residue Z is bondedto the group R by a single bond. The single bond can freely rotate inthe molecule so that the salt exhibits cationic conductivity by theaction of exchanging each other cations M^(k+) coordinated on theanionic residue Z.

In the formula I, the group R may have functional groups that can bepolymerizable. Further, the polymerizable functional groups areunsaturated bonds that are addition-polymerizable. The group R may be apolymer of organic group having addition polymerizable unsaturatedbonds. The group Q in formula I may be an aryl group. Further, informula I, the group Q is an aryl group, Z− may be a hydroxyl residue,and M+ may be lithium ions.

The formula of the polymer encompasses the compounds (2), (3) and (4)shown below:

wherein R_(p) is an organic group of an m valences is an integer of 1 or2, X is an organic group and m is an integer of 1 or more.

wherein R_(p) is an organic group of an m valences is an integer of 1 or2, and m is an integer of 1 or more.

wherein R_(p) and m are as defined previously.

The organic group R is not limited in the present invention; there are,for example, saturated hydrocarbons, unsaturated hydrocarbons, aromatichydrocarbons, etc. The group may contain not only pure hydrocarbons, butalso groups of hydrocarbons substituted with nitrogen, sulfur, oxygenatom, halogen atoms. Molecular weight of the groups is not limited;there are low molecular weight compounds to high molecular weightcompounds. The high molecular weight compounds may be polymers of low orhigh molecular weight monomers.

The number of substitutes of the organic group Q is not limited; thenumber of one or more per one molecule is sufficient. When the group Ris the polymer, the number may be that corresponding to the degree ofpolymerization. Further, several kinds of polymerizable monomers may beused to substitute the group Z. Methods of polymerization are notlimited; for example, addition polymerization, addition polyaddition,polycondensation, etc. may be employed.

The group Z is a group having a function capable of coordinating cationsthereon; when the group Z is oxygen (O⁻), the group Q may be phenolateanions such as hydroxylphenyl group, dihydroxylphenyl group, etc.

When the functional group Z is methoxy group (—OCH₃), there arealkoxyphenyl groups such as methoxyphenyl, dimethoxyphenyl, etc.However, the functional groups should be methoxy group and ethoxy groupas alkoxy group. If the number of carbon atoms is too large, it mayinterfere the rotation of the single bond or it may adverse affect onthe solubility of the cationic conductor to make worse workability ofthe material.

Other groups of which oxygen is substituted with sulfur, such asthiophenyl group or dithiophenyl group may be employed. Other functionalgroups may be ester(-O—C(═O)—R⁶, —C(═O)—R⁷), amino group (—NR₁R₂), acylgroup(—C(═O)—R⁸), carbonate group(—O—C(═O)—OR⁹), etc. R⁶—R⁹ are allalkyl groups.

The functional groups must be bonded by a single bond to the group R.Among the various compounds, the most preferable compounds are the groupR is bonded to the group Q through an amide bond.

Cations used in the present invention include ions of alkali metals suchas lithium, sodium, potassium and ions of alkaline earth metals such asmagnesium, etc. Among the above ions lithium ions are most preferable.

The lithium ion conductive polymer of the present invention can be usedas a separator, as well as an electrolyte. The polymer functions aselectrolyte and separator. The polymer is formed in sheet of a thicknessof several micrometers. The polymer can also be used as an anode towhich positive active materials are added for lithium ion batteries.

In lithium batteries, positive active materials are LiCoO₂, LiNiO₂,Li_(1+x)Mn_(2−x)O₄ (x=0˜0.33), Li_(1+x)Mn_(2-x-y)M_(y)O₄ (M is a metalwhich is selected from Ni, Co, Cr, Cu, Fe, Al, Mg, x=0˜0.33, y=0˜1.0,2-x-y>0), TiS₂, MoS₂, V₆O₁₂, VSe, NiPS₂, polyaniline, polypyrrole,polythiophene, etc.

Negative active materials are graphite or carbon in which lithium ionsare intercalated in the lamellar structure, lithium metal, lithium-leadalloy, etc.

Description of the Preferred Embodiments EXAMPLE 1

232 Grams of salicylic acid and 283 grams of 1-hydroxybenzotriazole werecompletely dissolved in a mixed solvent consisting of 3 dm³ oftetrahydrofuran and 2.5 dm³ of N,N′-dimethylformamide, the solventhaving been dried by evaporation. The solution was stirred at roomtemperature for 30 minutes.

The solution was then cooled to zero ° C., and 287 grams of1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide was dropped in thesolution, followed by stirring at zero ° C. for 30 minutes. To thesolution slowly dropped was 2 dm³ of tetrahydrofuran containing 245grams of vinylaniline and cooled to zero ° C., followed by stirring thesolution at room temperature for 2 days.

The reaction solution was condensed to extract an ethyl acetate phasefrom ethyl acetate and hydrochloric acid of 2 normals. The extract wasrinsed with hydrochloric acid and saturated sodium chloride solution anddrying with sodium sulfate, followed by condensation and purification toobtain white powdery solid.

Intermediate I; N-(4-vinyl phenyl)-2-hydroxy-benzoic amide

50 Grams of the resulting solid was completely dissolved in 1 dm3 oftetrahydrofuran, and 46 cm³ of 10M n-hexane solution of butyl lithiumwas dropped in the solution, followed by stirring. The solution wascondensed and the resulting substance was cast on a sheet ofpolytetrafluoroethylene. The film was dried under reduced pressure atroom temperature to produce a cast film having a thickness of 100micrometers.

The cast film was sandwiched between electrodes made of stainless steel(SUS 304) each having a diameter of 15 mm to obtain a cell forevaluation.

An amplitude voltage of 10 mV was applied to the cell at roomtemperature to measure a. c. impedance. A frequency range was from 1 Hzto 1 MHz. An ionic conductivity was derived from the reciprocal numberof the bulk ohmic value that was obtained from measurement of the a. c.impedance. The ionic conductivity was 5×10⁻⁴ Scm⁻¹, which was largerthan that of the solid electrolyte made of polyethyleneoxide.

EXAMPLE 2

259 Grams of dihydroxybenzoic acid and 283 grams of1-hydroxybenzotriazole were completely dissolved in a mixed solventconsisting of 3 dm³ of tetrahydrofuran and 2.5 dm³ ofN,N′-dimethylformamide, the solvent having been dried by evaporation.The solution was stirred at room temperature for 30 minutes.

The solution was then cooled to zero ° C., and 287 grams of1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide was dropped in thesolution, followed by stirring at zero ° C. for 30 minutes. To thesolution slowly dropped was 2 dm3 of tetrahydrofuran containing 245grams of vinylaniline and cooled to zero ° C., followed by stirring thesolution at room temperature for 2 days.

The reaction solution was condensed to extract an ethyl acetate phasefrom ethyl acetate and hydrochloric acid of 2 normals. The extract wasrinsed with hydrochloric acid and saturated sodium chloride solution anddrying with sodium sulfate, followed by condensation and purification toobtain white powdery solid.

Intermediate II; N-(4-vinyl phenyl)-2,6-dihydroxy-benzoic amide

50 Grams of the resulting solid was completely dissolved in 1 dm³ oftetrahydrofuran, and 46 cm³of 10M n-hexane solution of butyl lithium wasdropped in the solution, followed by stirring. The solution wascondensed and the resulting substance was cast on a sheet ofpolytetrafluoroethylene. The film was dried under reduced pressure atroom temperature to produce a cast film having a thickness of 100micrometers.

The cast film was sandwiched between electrodes made of stainless steel(SUS 304) each having a diameter of 15 mm to obtain a cell forevaluation.

An amplitude voltage of 10 mV was applied to the cell at roomtemperature to measure a.c. impedance. A frequency range was from 1 Hzto 1 MHz. An ionic conductivity was derived from the reciprocal numberof the bulk ohmic value that was obtained from measurement of the a.c.impedance. The ionic conductivity was 4×10⁻⁴ Scm⁻¹, which was largerthan that of the solid electrolyte made of polyethyleneoxide.

EXAMPLE 3

356 Grams of 2,6-dimethoxybenzoic acid was completely dissolved in 1 dm3of vaporization-dried N-methyl pyrrolidone. To the solution added were280 ml of triethylamine, 805 grams of(2,3-dihydro-2-thioxo-3-benzolyl)phosphonate and 260 ml of aminostyrene.The solution was stirred at room temperature for one day. The reactionsolution was dropped in 8 dm3 of aqueous solution of 1% sodiumhydrogencarbonate, and then the solution was stirred. The precipitatedsolid was purified with ethylacetate/n-hexane to obtain solid.

Intermediate III; N-(4-vinylphenyl)-2,6-dimethoxy benzoic amide

140 Grams of the resulting solid was completely dissolved in 5 dm3 oftetrahydrofuran, and then 0.4 gram of azobisisobutylonitrile was added.The solution was stirred at 65° C. The reaction solution was dropped in10 dm³ of n-hexane to obtain polymer. 50 Grams of the polymer wascompletely dissolved in 2 dm³ of N-methyl pyrrolidone, and then 98 gramsof lithium trisulfoneimide was added to the polymer solution and thesolution was stirred. The polymer solution was cast onpolytetrafluoroethylene sheet and the cast film was dried at 60° C. invacuum to obtain cast film of 100 μm thick.

The cast film was sandwiched between a pair of stainless electrodes(SUS304) of 15 mm diameter to prepare a cell for evaluation. A.C.current of amplitude of 10 mV was applied to the cell at roomtemperature to measure A.C. impedance. The range of frequency was from 1Hz to 1 MHz. An ionic conductivity was determined from an inverse of abulk resistance obtained from the A.C. impedance. The ionic conductivitywas 1.4×10⁻⁴ Scm⁻¹, which was almost the same as that of the solidelectrolyte that used polyethylene oxide.

In FIG. 2 there is shown a sectional view of a lithium battery that usesthe polymer electrolyte obtained in the above procedure. In FIG. 1 thereis shown a graph that shows relationship between ionic conductivity ofthe polymer electrolyte and temperatures.

The electrolyte obtained in this example exhibits a very smalltemperature coefficient, compared to one obtained in Comparative Ex.That is, the coefficient of the electrolyte of Example 3 at −20° C. isalmost the same as that at room temperature.

However, the electrolyte obtained in comparative 2 shows a temperaturecoefficient change resulting in that ionic conductivity decreases in theorder level as the temperature increases. Therefore, the electrolyte ofthe present invention exhibits much better ionic conductivity than thecomparative polymer electrolyte.

EXAMPLE 4

356 Grams of 2,6-dimethoxybenzoic acid was completely dissolved in 1 dm3of vaporization-dried N-methyl pyrrolidone. To the solution added were280 ml of triethylamine, 805 grams of(2,3-dihydro-2-thioxo-3-benzolyl)phosphonate and 260 ml of aminostyrene.The solution was stirred at room temperature for one day. The reactionsolution was dropped in 8 dm3 of aqueous solution of 1% sodiumhydrogencarbonate, and then the solution was stirred. The precipitatedsolid was purified with ethylacetate/n-hexane to obtain solid.

Intermediate IV; N-(4-vinylphenyl)-3,5-dimethoxy isonicotinamide

140 Grams of the resulting solid was completely dissolved in 5 dm3 oftetrahydrofuran, and then 0.4 gram of azobisisobutylonitrile was added.The solution was stirred at 65° C. The reaction solution was dropped in10 dm³ of n-hexane to obtain polymer. 50 Grams of the polymer wascompletely dissolved in 2 dm³ of N-methyl pyrrolidone, and then 98 gramsof lithium trisulfoneimide was added to the polymer solution and thesolution was stirred. The polymer solution was cast onpolytetrafluoroethylene sheet and the cast film was dried at 60° C. invacuum to obtain cast film of 100 μm thick.

The cast film was sandwiched between a pair of stainless steelelectrodes (SUS304) of 15 mm diameter to prepare a cell for evaluation.A.C. current of amplitude of 10 mV was applied to the cell at roomtemperature to measure A.C. impedance. The range of frequency was from 1Hz to 1 MHz. An ionic conductivity was determined from an inverse of abulk resistance obtained from the A.C. impedance. The ionic conductivitywas almost the same as that of the solid electrolyte that usedpolyethylene oxide.

EXAMPLE 5

183 Grams of 2,6-dimethoxybenzoicacid was completely dissolved in 500 mlof N-methylpyrrolidone that was evaporation-dried. Then, 140 ml oftriethylamine and 403 grams of(2,3-dihydro-2-thioxo-3-benzolyl)phosphonate were added to the solution.

The solution was added to 434 grams of tris(2-aminoethyl)amine that wasdissolved in 500 ml of N-methylpyrrolidone, while cooling the solution.The solution was stirred at room temperature for two days. The reactionsolution was dropped in 10 dm³ of aqueous solution of 2% sodiumhydrogencarbonate, and the solution was stirred. The precipitate wasextracted with ethylacetate/n-hexane to obtain a solid.

Intermediate V; N-(di(2-aminoethyl)aminoethyl)-2,6-dimethoxybenzoicamide

1.5 dm³ of carbon tetrachloride containing 183 grams of adipic aciddichloride was added to 1.5 dm³ of aqueous solution in which 160 gramsof the solid and 40 grams of sodium hydroxide were dissolved, whilestirring, thereby to precipitate polymer. 50 Grams of the resultingpolymer was dissolved in 2 dm3 of phenol, and then 58 grams of lithiumtrifluorosulfoneimide was added to the solution under stirring.

Then, the solution was cast on polytetrafluoroethylene sheet, and thecast film was dried under vacuum at 60° C. to obtain cast film of 100.μm thick. The cast film was sandwiched between a pair of stainless steelelectrodes (SUS304) of 15 mm diameter to prepare a cell for evaluation.

A.C. current of amplitude of 10 mV was applied to the cell at roomtemperature to measure an A.C. impedance. The range of frequency wasfrom 1 Hz to 1 MHz. An ionic conductivity was determined from an inverseof a bulk resistance obtained from the A.C. impedance. The ionicconductivity was almost the same as that of the solid electrolyte thatused polyethylene oxide.

EXAMPLE 6

148 Grams of 4-vinylbenzoicacid and 160 grams of 1-hydroxybenzotriazolewere completely dissolved in a mixed solvent consisting of 2 dm3 oftetrahydrofuran and 1.5 dm³ of N,N′-dimethylformamide, and the solutionwas stirred at room temperature for 30 minutes. The solution was cooledto 0° C., and then 171 grams of1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide was dropped, and it wasfurther stirred at 0° C. for 30 minutes.

To the solution dropped was 2 dm³ of tetrahydrofuran being cooled to 0°C. and containing 138 grams of 2,6-dihidroxyaniline gradually. Thesolution was stirred at room temperature for two days. The reactionsolution was condensed and ethyl acetate phase was extracted from 2normal hydrochloric acid.

The extract was rinsed with hydrochloric acid and saturated sodiumchloride solution, and then was dried with sodium sulfate. The productwas condensed and purified to produce white solid.

Intermediate VI; N-(2,6-dihydroxyphenyl)-4-vinyl-benzoic amide

50 Grams of the resulting solid was completely dissolved in 1 dm³ oftetrahydrofuran, and then 46 cm3 of 10M hexane solution of butyl lithiumwas dropped in the solution under stirring. The solution was condensedand cast on polytetrafluoroethylene sheet. The cast film was dried atroom temperature to obtain cast film of 100 μm thick. The cast film wassandwiched between a pair of stainless steel electrodes (SUS304) of 15mm diameter to prepare a cell for evaluation.

A.C. current of amplitude of 10 mV was applied to the cell at roomtemperature to measure an A.C. impedance. The range of frequency wasfrom 1 Hz to 1 MHz. An ionic conductivity was determined from an inverseof a bulk resistance obtained from the A.C. impedance.

The ionic conductivity was 1.6×10⁻⁵ Scm⁻¹, which was almost the same asthat of the solid electrolyte that used polyethylene oxide.

COMPARATIVE EXAMPLE

37 Grams of a copolymer consisting of 20 mole % of ethylene oxide and2-(2-methoxy) ethylene glycidylether and 6.6 grams of LiPF6 as anelectrolyte salt were mixed, and the mixture was dissolved inacetonitrile to prepare a solution. The solution was cast on apolytetrafluoroethylene sheet, and the cast solution film was driedunder reduced pressure at 80° C. to obtain a cast film of a thickness of100 micrometers.

The cast film was sandwiched between electrodes made of stainless steel(SUS 304) each having a diameter of 15 mm to prepare a cell forevaluation. An amplitude voltage of 10 mV was applied to the cell atroom temperature to measure a.c. impedance. A frequency range was from 1Hz to 1 MHz. An ionic conductivity was derived from the reciprocalnumber of the bulk ohmic value that was obtained from measurement of thea.c. impedance. The ionic conductivity was 5×10⁻⁵ Scm⁻¹.

As having been described in Examples and Comparative Example, the solidelectrolyte according to the present invention that exhibits ionicconductivity mechanism based on the single bond rotation showed higherionic conductivity than the conventional solid electrolyte whoseconductivity is based on segmental motion of molecular chains.

The polymer of the present invention can be used as an electronicconductive material for connecting unit cells of a fuel cell system,capacitors, etc.

1. A lithium battery comprising an active positive material, an activenegative material and a solid electrolyte, wherein the electrolyte is apolymer represented by the general formula,

wherein R_(p) is a residue of a polymer of a compound having apolymerizable unsaturated bond, Q is an organic residue of n+1 valencesand connected through an amide group to R_(p) by means of a single bond,M^(k+) is a cation of k valence, Z is an organic function group capableof forming an ionic bond with cation M^(k+) or an organic function grouphaving a coordination capability with M^(k+), and m, n and k areintegers of one or more.
 2. The lithium battery according to claim 1,wherein Q is a six-membered ring, and wherein Z is connected to a carbonatom in the six-membered ring, the carbon atom to which Z is connectedbeing next to the single bond.
 3. The lithium battery according to claim1, wherein R_(p) is a residue of a copolymer of an aryl compound andanother compound.
 4. The lithium battery according to claim 1, wherein Qis an aryl group connected through the amide group to R_(p) by means ofa single bond.
 5. The lithium battery according to claim 1, wherein Q isa six-membered ring.
 6. The lithium battery according to claim 1,wherein R_(p) is a residue of polystyrene.
 7. The lithium batteryaccording to claim 1, wherein the polymer is represented by the formula(2)

wherein X is an amide group.
 8. The lithium battery according to claim1, wherein the polymer is represented by the formula (3):


9. The lithium battery according to claim 1, wherein the polymer isrepresented by the formula (4):


10. The lithium battery according to claim 1, wherein R_(p) is a residueof polystyrene, each of the groups (Q(Z⁻ . . . M^(k+))_(n))_(m) ispendent from a styrene unit through an amide group, Z is hydroxyl groupor methoxy group, and M^(k+) is lithium ion.
 11. The lithium batteryaccording to claim 1, wherein said polymer is made from an intermediateof said polymer, which is represented by the general formula:


12. The lithium battery according to claim 11, wherein Q is an organicgroup of a six-membered ring connected through the amide group by meansof a single bond to R.
 13. The lithium battery according to claim 11,wherein Q is an aryl group connected through the amide group to R. 14.The lithium battery according to claim 11, wherein R is a residue ofstyrene.
 15. The lithium battery according to claim 12, wherein Z isconnected to a carbon atom in the six-membered ring, the carbon atombeing next to the single bond.
 16. The lithium battery according toclaim 11, wherein Q is a six-membered ring connected through the amidegroup to R.